Guest guest Posted July 9, 1999 Report Share Posted July 9, 1999 Welcome Chris: And you are very savvy checking things out so soon after being diagnosed. HMO, I can relate, no one watching you or caring about you....been in that living void for years now. I am new as well, so far tons of my questions have been answered without even having to ask them! It is a great thing to find others going through it as well, isolation is not good. You have to get aggressive with the doctors and ask questions, and write down the answers cause if you are anything like me right now, you won't understand what they are saying. We will learn as we go! I found that this disease is progressive, so finding out how to change things in your life like has posted we may again feel normal! You have a great opportunity for change and relief early in the game! :-) Froglady <862567a8.0079c83c.0-@...> wrote: original article:hyperthyroidism/?start=24 51 Hi. I'm new to this, just diagnosed with Hyperthyroidism. It seems quite mild, given the e-mails and chats I've been reading and more telling, that my uptake was relatively close to normal although still out of whack. How does this group work? Is it a place to ask questions? I'm on HMO care so I feel that no one is monitoring my situation, and I'd better get savvy and do it myself. Thanks for any input. I. ------------------------------------------------------------------------ eGroups.com home: hyperthyroidism - Simplifying group communications Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2001 Report Share Posted May 10, 2001 Hi Mark! Welcome to Longevity! This discussion list has been fairly inactive lately, mainly because the primary instigator of debate and controversy (yours truly) has been active in other health-related message forums. If I may ask, what anti-depressants are you taking? Also are you taking any vitamins and health supplements? -gts (Gordon) > New Guy > > > Hello, > My name is Mark and I'm a new guy. I'll get the bio out of the way. > Age 42, from North Carolina, USA, Occupation - Inventor/Businessman, but > trying to come out of retirement that was forced by my last injury to an > already banged up spine. Two years on Methadone that I can > barely remember > and another two on various Pain meds that have been hell. I've > almost lost > my wife but at the moment am still married, three wonderful kids who don't > deserve any of the strife from this. Through my own research for help > regarding my spine I found that one of the side effects of the > meds was loss > of testosterone and have been getting monthly injections for two > years. (1 > cc of 200 mg/ml per month) Good results and this is a part of > the reason I > am doing so much better along with anti depressants, an excellent > chiropractor and a pain management doctor who worked with me on > finding the > right medicine (Opiates) and dose to control my pain and minimize the side > effects. > I am very involved with international work and just returned from > India where I found Testosterone over the counter in 1 cc ampoules > (250mg/ml) for not very much money at all. Been actively researching HGH > over past month and am now about to get my first round of test through the > Hilton Head Island Clinic. Very nice gentleman named Lazarus Long > recommended I call them. I am hoping to take advantage of my contacts in > these other countries to lower the cost of the HGH I almost certainly will > be taking. I have a good friend returning to the us in just a > few days and > am trying to get prices from him. I told him to inquire about " Somatrin " > and fear he will hit a language barrier without a specific medicine to > request. If I knew more I could possibly be getting 50 or 100 IUs in > transit just anticipating the need for it. Travel time will be a > few weeks > since they aren't coming directly home and I should have test results back > by then but it will be too late to take advantage of this courier. Any > Suggestions? > BTW, I'm of slightly above average height at 6'2 and a little over > weight (240 lbs) due in large part to the slower metabolism > associated with > the narcotics. I exhibited most of the GH deficiency characterizes long > before the spine injury from depression to all the other mental effects in > addition to degenerative disk disease and what the surgeons call " failed > spine syndrome " . In other words " it's all messed up and be happy your not > in a wheelchair! " I will provide some dialogue on my opinions > and look for > others regarding hormone deficiency associated with Chronic pain and would > really welcome the input of others. > I'll try to be a courteous list member and thank you all in advance > for humoring me. I am a man of Faith so don't expect any dirt from me but > don't think you can't be yourself while I'm involved either. > Thanks, > Mark A > 5-10-01 > 9:50 pm edt > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 24, 2001 Report Share Posted June 24, 2001 In a message dated 6/23/2001 12:12:09 PM Eastern Daylight Time, mark_anthonyau@... writes: > > I was hoping to get some feedback from others here, the results they > have had from following the plan. > The book by Dr D'adamo cites two examples of dramatic > improvements in t-cell counts and overall condition An increase in t-cells is not an improvement in health. It is a response to an increase in toxicity in the body. Any doctor who treats " the virus " is a quack or a misinformed fool who is just following orders and watching his patients die. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2001 Report Share Posted September 9, 2001 Welcome to the List Ed, Nice to have you onboard, and thank you for taking the time to to introduce yourself, Best Wishes Ian Listowner __________________________________________ Ian Sharpe International SOS Paramedic AGIP Kco Marine Supply Base Bautino, Republic of Kazakhstan Tel: +31 70 313 3655 / 3690 (Clinic/ Accomodation) -------------------------------------------------------------------------- Personal Mail to Ian@... New Guy Hi My intrest in out of hospital care began as a kid with the American Red Cross. I was an Army medic. Went to school, an now an emergency physician in Florida. Am combat medic, flight surgeon, fire surgeon and work with SAR. My roots are as a remote site medic, thats why I requested membership. Ed Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 7, 2001 Report Share Posted November 7, 2001 Hi, Terry, and welcome! looking for any info/things I should know about Social Security Disability applications. I have my first appointment with one of their (Social Security's) Drs tomorrow. TIA..... Oh boy. First advice: go to that appointment, and then hire yourself an attorney when you get the feedback from them. It's pretty difficult to qualify on the first git-go. My husband is the ICD guy around here. He had to get a lawyer to qualify for disability, and that was BEFORE his implant. The good news is that the lawyer doesn't cost you anything.... there are tons of 'em who'll take on SSA and come out ahead, and they just get a percentage of your back award money. Welcome to a great group. Sue -- "She was not quite what you would call refined. She was not quite what you would call unrefined. She was the kind of person that keeps a parrot." -- Mark Twain Rich and Sue Owens http://www.geocities.com/Yosemite/Meadows/7457/index3.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 8, 2001 Report Share Posted November 8, 2001 Terry, I had to apply for social sec. disability and then had to appeal it once and thenI got it. I didn't have to get a lawyer but I do know that a lot of people have to get one. I think if your doctor is strong on saying you are not able to work....that helps a lot. Also my ejection fraction was 25%. I think that helped me to get it also. Good luck. Ruth in PA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 8, 2001 Report Share Posted November 8, 2001 You sure do and welcome. Tell us a little about yourself. We are all great listeners. Bill is the witt, Bob is the captain of the boat and me well I am not sure what I am besides crazy and wired for zapping. Sharon in Ohio Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 8, 2001 Report Share Posted November 8, 2001 Well, here I go throwing my two cents worth in. I had no trouble getting my disability. It took six months but all I had to do was fill out the paper work submit it and then go to all those crazy appointments and have a visit with a shrink. I think that did it for me they thought this lady is hopeless. I did not have to use an attorney but I know that others have had to. I got my disability the first time around wit no hassle except for the wait and seeing the shrink which took three hours. Sharon in Ohio Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 8, 2001 Report Share Posted November 8, 2001 I agree about getting a lawyer ... might as well do so from the get go... I attempted to go about it on my own first yr... was waste of my time... then when I finally got lawyer, got approved w/out his help, let him go, then had review beginning 2 wks later, lost benefits w/in next year ... was the most stressful 2 yrs of my life... wouldn't wish it on my worst enemy... good luck to you and welcome to the 'board. JES in NJ... God Bless America > Hi all, > Terry here from Long Island NY, Had a bunch of stents (7) put in last > April then an AICD 2 weeks ago. Do I qualify for membership on the > list? My REAL e-mail is Harlyred1@a... " e " in HarlEy....I'm > looking for any info/things I should know about Social Security > Disability applications. I have my first appointment with one of > their (Social Security's) Drs tomorrow. TIA..... > Terry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 13, 2002 Report Share Posted May 13, 2002 Hi , welcome. I may not be of much help, but many people here are eating low glycemic diets, free from carniferous (sp?)vegetables (broc., cauli, etc). I would stay away from fluoride as much as possible and take a good multivitamin. best wishes ----Original Message Follows---- From: " robert andrew " <mommyb@...> Reply-hypothyroidism <hypothyroidism > Subject: NEW GUY Date: Mon, 12 Aug 2002 03:45:31 -0400 greetings, all. new guy, here. i am beginning research on hypothroidism, since my doc said i am borderline. my first problem is that i cant determine if eating too much fish can cause ht, or if eating a lot of fish can help correct the imbalance. any comments appreciated. secondly, there are scores of website on the net on this subject, but i am specifically looking for ways to exclusivley use diet to treat onset borderline ht. again, any comments would be appreciated. and lastly...what is the best place on line for good reliable information on this subject, that goes in depth? again...thanking you in advance for your help. i pray good health to you all robert Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 13, 2002 Report Share Posted May 13, 2002 , I'm sure someone has the easy way into this website for you, but you can go to www.about.com and type in hypothyroid in the search window. Look for Shomon's site. It has alot of good, easy to understand info. on it. Good luck Love and take care, Reneé and Jerry rja86@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 22, 2002 Report Share Posted May 22, 2002 , Actually, fluoride is one of those essential trace elements which is necessary for good health. Fluoride is especially beneficial for middle-aged and older women as it helps prevent osteoporosis. Please see http://content.health.msn.com/content/article/1671.53264 for more details. Celeste Pierce wrote: > I would stay away from fluoride as much as possible and take a > good multivitamin. best wishes > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2002 Report Share Posted September 18, 2002 JEREMY, I had a C5-6 fusion. Still in a great deal of pain most of the time. Suicide would be easier. If you want to talk write me @ raaron69@... Cya, Rich Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2003 Report Share Posted March 2, 2003 Straun, Welcome to the list. Gareth >From: Struan Reid <areid3@...> >Reply- > >Subject: New Guy >Date: Sun, 02 Mar 2003 15:58:50 +0300 > >Hi, > >Name: Struan Reid > >Age: 30 > >Nationality: South African > >Qualification: National Diploma Ambulance and Emergency Care (SA) > ACLS > ATLS > Advanced Rescue > >Current Job: Remote ALS Paramedic for a land seismic exploration company in >Saudi Arabia. > >Previous Job: Remote ALS Paramedic, Medical Rescue International - >Mozambique > >Interests: Diving; Land Rovers; Rescue and ALS. > >Hello to all out there, > >Struan > > _________________________________________________________________ Chat online in real time with MSN Messenger http://messenger.msn.co.uk Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2003 Report Share Posted March 3, 2003 Hi Struan welcome to the list - nice to know that there are other landy lovers out there! - best 4x4 by far...! enjoy the banter! best wishes New Guy Hi, Name: Struan Reid Age: 30 Nationality: South African Qualification: National Diploma Ambulance and Emergency Care (SA) ACLS ATLS Advanced Rescue Current Job: Remote ALS Paramedic for a land seismic exploration company in Saudi Arabia. Previous Job: Remote ALS Paramedic, Medical Rescue International - Mozambique Interests: Diving; Land Rovers; Rescue and ALS. Hello to all out there, Struan Member Information: List owner: Ian Sharpe Owner@... Editor: Ross Boardman Editor@... Post message: egroups Subscribe: -subscribeegroups Unsubscribe: -unsubscribeegroups Thank you for supporting Remote Medics Online. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 21, 2003 Report Share Posted May 21, 2003 Hi , nice to meet you. My name is . I have Fibromyalgia, & probable Lupus (seems to depend on which dr I see & when), and a couple of other things that keep life interesting. Sometimes I can power thru it, and sometimes.... well, you just get sick & tired of being sick & tired! Sorry you're having a rough time. I think you need more than a month to get over just about any surgery, and it may take you longer, cause this isnt the first time your body's been assaulted lately, right? I've checked with a bunch of them drs, and not a one of em has a magic wand. Darn it. We've got all kinds of good people here, from all over, that have been so much help, to me and each other. And the medical info is remarkable, so ask away. So what kind of meanness have you been through? Hope we can help. > > I just joined this group this morning, and read a few of the last > posts before I tossed a hello post out here- > > I found the group while searching for another (specific) kind of > support/info group, and I think it might have dropped in my lap at > just about the right time- who knows. I've been really having a hard > time of things only the last few weeks, even though I have been > chronically ill for a few years now. (including this past year or so, > undergoing multiple surgeries and such- it sucks.) ...but for some > reason, I am just not handling right NOW very effectively. I have no > idea why... I just feel like I can't quite bounce back, when I really > should be able to, you know? > > Anyway, here I am, eh? (grin) I feel kind of funny just posting all > the medical BS I recently went through, especially since really, I > should be at the END of the proverbial tunnel physically, and getting > better now- but for whatever reason, my body hasn't read the > schedule, I guess. Maybe if i'm lucky it'll be a phase I will get > over. The last surgery was more than a month ago, so you'd think it'd > be about flipping time. :/ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 21, 2003 Report Share Posted May 21, 2003 I think you need more than a month > to get over just about any surgery, and it may take you longer, cause > this isnt the first time your body's been assaulted lately, right? > I've checked with a bunch of them drs, and not a one of em has a > magic wand. Darn it. We've got all kinds of good people here, from > all over, that have been so much help, to me and each other. And the > medical info is remarkable, so ask away. > So what kind of meanness have you been through? I guess I'm impatient, because I have always had such a strong healing system- although ironically, my Doctor has discussed my case with many collegues, and they all seem to think that is, in a strange way, what's causing/caused it. UGH... lemme see if I can make this make a little sense here- my apologies ahead of time for the length and topic- it's tough to line out as it is, much less without specifics. (sigh): I started getting really sick a couple years ago, when I was otherwise in a great frame of mind/body- i'd just gone back to college and was really doing smashing (I work in art, but I was really making the non-art grades, surprisingly- I even got inducted into Phi Theta Kappa for the work I was doing- I felt pretty darn good!)- It started with gut-problems (I figured maybe I was over- working, who knows?) but the pain and symptoms got out of control FAST. I've got a high pain thresh-hold, so my general physician referred me to a specialist, because the symptoms (all lower gastrointestinal) were really taking it out of me- I turned all bloaty-lookin' and pale, my energy plummeted, and I was violently sick more often than not, including pain that was just crippling- NOT like me. Unfortunately, the doctor diddled around, and although he was treating me on what he called an " emergent " situation, the idiot went off on a honymoon (for a MONTH) and 'forgot' to hand my case to one of the other docs in his large practice- while he was gone, I ended up in the hospital, and was diagnosed with gallstones, and rushed into surgery. (They say it was obscene he 'missed' it, since the stones filled not just the gallbladder, but much of the liver ducting. I lost some ducting and a part of my liver when they removed the gallbladder, because it had all become gangrenous- It took a long hospital stay too- and worse, I almost kacked on the operating room table, just to give them all a good scare. UGH) ...I thought, hey, this resolves it, right? UH uh... didn't happen. (whimper) I kept getting sick, nothing dietary helped, and the pain, tho MUCH less now that the gallbladder was not an issue, was still crippling in that I couldn't even attend classes when it hit. I got a new general doctor (for an unrelated reason) and the new one was very concerned, and called around untill she got me the surgeon I have had for the past year or so now- I honestly can't say enough good things about him! He jumped RIGHT in on it, and dug untill he found answers... or as many as anyone could, which is where it starts getting murky/hard to understand. He found a tumor (that the other doc had apparently found and ignored because he didn't think it could cause that kind of pain) that had formed around a stricture in the sigmoid colon just at the rectum and sigmoid join. It was strangling the gut there, and probably causing all the 'sick' I was experiencing- The thing is, it didn't come up as true /cancer/... it was a fiberous tumor, but non-malignant... he snagged me into surgery, and removed it, just above and just below the stricture, which he called 'stenosis' or 'anastenosis'- this is about my level of understanding, that it was like 'concrete' in testure- I thought he was teasing a little, being exaggeratory, but no- it was almost calcified. Again, we figured that would resolve it, you know? But during the resection surgery, they couldn't locate a leak, and so created a temporary illeostomy. (isn't THAT a fun friend to wake up to? congrats, the tumor is gone, meet your new buddy, the illeostomy!) Everything kind of gets muddy for me after that, because I was coping with the temporary illeostomy, while we tried to figure out WHY the body reacted to the surgery by immidiately creating another stricture at the surgery point. ...more anastenosis. He thought maybe it was vascular, and so removed more sigmoid, and tried 'opening' it several times at various levels of surgery/anesthesia. No deal... it keps coming back... each time he lost a battle against a stricture, he was talking to other docs, tho- and I guess they all are about as baffled, and think maybe my body was trying to heal SO fast and hard, it was doing this, you know? It baffled me too, frankly. The last surgery to fix the stricture was pretty intense- he removed the sigmoid and much of the rectum, and ended up creating what was called a " colon pouch " (it's more commonly done with small intestine, not large- but in this case, with almost no 'storage space' between the colon and remaining retcum, he created the colon pouch to give me that space back- otherwise, i'd have been running to the bathroom every few minutes. UGH...) The colon pouch is created by doubling the colon onto itself and then snipping the divider and attaching the bottom of the " U " to the rectum- and the surgery went well and he reversed the illeostomy at the same time. Healing from THAT was slow! They leave the rather large hole in your belly (mine was about 3 " across and 2 " deep or so) and let it heal on it's own... but I heal fast, and that's where it is now- all healed but for the tiniest little scab and my now amazing collection of frankenstien-scars. (they run from the lowest point at the pubic bone to the highest point JUST under the breastbone. icky!) By all rights, it should be OVER. Done. Finito. ...There is a small section of stenosis, but it's less than 1/3 of the diameter of the surgery joint, so it isn't a problem enough to even mess with (lest that make it worse, you know?)... but even tho I was on my feet and home again in only a couple days, I just... I haven't come back. I'm starting to really feel it, too- the surgeries were hard but no biggie in the end... but that this didn't 'fix' everything... I just don't know what to do. A week or two after surgery, my gut was still going nuts, but you know, it had been disconnected for almost a year! ...so I was cutting that some serious slack, and not worrying... except I am just exhausted... sleep all the time, NO joke- or can't sleep at all. Nothing in between. I took a 'trazodone' on doctors orders to get some sleep after an insomnia, and I slept for three days, with only two half-our wake periods per day... hey, I like sleep, but... YIKES. No more of those! I sleep too much, even with the times I 'can't get to sleep when I want to' and I am just exhausted all the time. I feel like I have been beat on- my gut gives me a one minute warning before everything has to go or ELSE (I think the pouch fills, and then the uh, you know, potty emergency is just taking it out of me when that happens) yet again- that too is sucking the life out of me like the illeostomy never did!! (and with the illeostomy, I was so badly dehydrated once, I had a 20 day hospital stay while they got me back again! argh!) ...I sweat profusely or get shivery-cold with very little 'reason'. It doesn't seem to matter what the external temp is, my body is just going off on me, you know? I KNOW it's only been a month or so- I had the pouch/takedown surgery in the first week of April- but the whole 'being sick' thing never happened before, with all the other surgeries! I bounce back quick! ...this time... it's been hellish. My gut STILL goes nuts like this, and that has created a world of pain from hemmrhoids/fissures caused only by that irritation... I'm really having the worst time of it emotionally, because there's so many issues to think about, you know? I REALLY expected this was the 'solve' and it'd be over and done with... and before the last couple surgeries, my surgeon stopped taking the medicaid/DSHS I am stuck on, and was doing the work for free/gratis, only because he felt he'd " started it " and wanted to be the one to finish it and see me through- his attitude twords me never changed, but BOY did his office's!! ...I couldn't hardly talk to the receptionest without getting a grilling- all because I was essentially a charity case, without a way to pay... I know I can't call the office now, and go " back " , because not only would he struggle with it ethically (I'm sure anyway) but the office gal would make me crazy. I'm not an ego- type, but my pride is battered enough with the indignancy of this whole thing as it IS... this is not a fun part of the anatomy to have everyone focused on, heh!... but I can't handle this whole charity thing... it was just the final straw internally, when the problems didn't resolve. The last follow-up I had, he didn't expect any more problems, and handed me back to my general doc. The only thing is, it's been a couple weeks, and I am still REALLY suffering, and I just don't know what I should do. It's complicated- he was treating me gratis for the last bit in part because he was training a new " fellow " (surgeon coming into this specialty) and that guy is (apologies to any who might know him!) kind of a jerk. I just don't much like him, or i'd go pester HIM... but now that I am supposed to be done, and over with and everything... I don't really know how to cope with this still being a problem. I AM giving it some time, in hopes it is just everything learning how to work again (i'm sure potty-training wasn't fun the first time, why would anyone want to experience the joys of that as a 30- something'er? smirk!) ...but because I am so out of it sick too.... I just really worry that there is still something wrong... and I don't have the slightest idea how to resolve it, who to go to, or even how to handle it mentally. A LOT of folks who have 'temporary' illeostomies end up having to get one for life, and i'm not too big on that idea, frankly... tho I wouldn't die or anything if it was the only way to fix things... but while cutting a PEICE of colon (or even all the sigmoid/ect) is a big deal, I am REALLY hesitant to let them yank out the whole colon... and typically, when they do that, they don't leave everything connected, they do the permenant illeostomy... sigh. ugh. argh... So that's the HUGEly long and confusing story... there's just no polite terms for it all... but I'm running in circles inside, worrying about what I am going to do now... especially if this doesn't all settle out in the next month or so. I can't spend the rest of my life laying in bed or on the couch because I can't sit up, you know? I was that sick before... and sleeping all the time is a definate quality-of-life killer too. (smirk) ...sleep is fun, but... argh!! ...and of course, like everyone else in the world, my personal life didn't stop for the duration, so I have the kinds of regular problems a lot of folks in my position have- things that I know I could handle better if I wasn't feeling so darn SICK all the time!! I haven't the slightest idea where to turn next... or how long to wait before I try and take action, you know? How much is too much? When is it /really/ being sick and not just being whiney, pushing too hard too soon.... and am I just somehow addicted to being sick all the time or something wierd like that? (I have NO idea why that scares me, but it does. I have always hated being sick, and so far as I can tell i STILL lothe it- but what IF... you know? people have gotten addicted to wierder!) ...bah. (hey, anyone still reading definately has my respect- that is some serious spammage there!) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 29, 2003 Report Share Posted May 29, 2003 Hi , how are you doing today??? Welcome to the group... You sure do have a lot to deal with... Please keep us posted... Welcoming Hugs Helen (hey, anyone still reading definately has my respect- that is some serious spammage there!) "Don't be afraid to be yourself. You are unique and special just the way you are." Sue Calwell & ((((((( RAINBOW HUGS ))))))) LOVE angelbear1129@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 5, 2003 Report Share Posted June 5, 2003 , Sorry for the slow reply, but hey, better late than never, right? You are *not* being whiny! Looking at your story from my perspective (and I only have measly IBS and hemmrhoids) you deserve a medal for your patience and what you've been through! I have more than a few choice words for that doctor that took you on gratis...that doesn't mean he (or his office personnel) can treat you like a second-class citizen. Many of us deal with the " am I just being a pain " syndrome, or " being sick addiction " syndrome (which neither exist) because you are a biological being and medical maladies happen...we don't cause them (with a few exceptions, mostly mental health related). Medical science isn't perfect by far, but hearing your doc's approach of " cut some now, cut some later, it aint' my colon " approach seems inhuman. Any doctor that does not take in to consideration your quality of life after their so-called treatment is going against the Hippocratic oath. Please update us...I'd like to know what the status is of this. Oh....BTW, I used to take care of a man with a colostomy....I have much respect for you. Hugs, Re: New Guy I think you need more than a month > to get over just about any surgery, and it may take you longer, cause > this isnt the first time your body's been assaulted lately, right? > I've checked with a bunch of them drs, and not a one of em has a > magic wand. Darn it. We've got all kinds of good people here, from > all over, that have been so much help, to me and each other. And the > medical info is remarkable, so ask away. > So what kind of meanness have you been through? I guess I'm impatient, because I have always had such a strong healing system- although ironically, my Doctor has discussed my case with many collegues, and they all seem to think that is, in a strange way, what's causing/caused it. UGH... lemme see if I can make this make a little sense here- my apologies ahead of time for the length and topic- it's tough to line out as it is, much less without specifics. (sigh): I started getting really sick a couple years ago, when I was otherwise in a great frame of mind/body- i'd just gone back to college and was really doing smashing (I work in art, but I was really making the non-art grades, surprisingly- I even got inducted into Phi Theta Kappa for the work I was doing- I felt pretty darn good!)- It started with gut-problems (I figured maybe I was over- working, who knows?) but the pain and symptoms got out of control FAST. I've got a high pain thresh-hold, so my general physician referred me to a specialist, because the symptoms (all lower gastrointestinal) were really taking it out of me- I turned all bloaty-lookin' and pale, my energy plummeted, and I was violently sick more often than not, including pain that was just crippling- NOT like me. Unfortunately, the doctor diddled around, and although he was treating me on what he called an " emergent " situation, the idiot went off on a honymoon (for a MONTH) and 'forgot' to hand my case to one of the other docs in his large practice- while he was gone, I ended up in the hospital, and was diagnosed with gallstones, and rushed into surgery. (They say it was obscene he 'missed' it, since the stones filled not just the gallbladder, but much of the liver ducting. I lost some ducting and a part of my liver when they removed the gallbladder, because it had all become gangrenous- It took a long hospital stay too- and worse, I almost kacked on the operating room table, just to give them all a good scare. UGH) ...I thought, hey, this resolves it, right? UH uh... didn't happen. (whimper) I kept getting sick, nothing dietary helped, and the pain, tho MUCH less now that the gallbladder was not an issue, was still crippling in that I couldn't even attend classes when it hit. I got a new general doctor (for an unrelated reason) and the new one was very concerned, and called around untill she got me the surgeon I have had for the past year or so now- I honestly can't say enough good things about him! He jumped RIGHT in on it, and dug untill he found answers... or as many as anyone could, which is where it starts getting murky/hard to understand. He found a tumor (that the other doc had apparently found and ignored because he didn't think it could cause that kind of pain) that had formed around a stricture in the sigmoid colon just at the rectum and sigmoid join. It was strangling the gut there, and probably causing all the 'sick' I was experiencing- The thing is, it didn't come up as true /cancer/... it was a fiberous tumor, but non-malignant... he snagged me into surgery, and removed it, just above and just below the stricture, which he called 'stenosis' or 'anastenosis'- this is about my level of understanding, that it was like 'concrete' in testure- I thought he was teasing a little, being exaggeratory, but no- it was almost calcified. Again, we figured that would resolve it, you know? But during the resection surgery, they couldn't locate a leak, and so created a temporary illeostomy. (isn't THAT a fun friend to wake up to? congrats, the tumor is gone, meet your new buddy, the illeostomy!) Everything kind of gets muddy for me after that, because I was coping with the temporary illeostomy, while we tried to figure out WHY the body reacted to the surgery by immidiately creating another stricture at the surgery point. ...more anastenosis. He thought maybe it was vascular, and so removed more sigmoid, and tried 'opening' it several times at various levels of surgery/anesthesia. No deal... it keps coming back... each time he lost a battle against a stricture, he was talking to other docs, tho- and I guess they all are about as baffled, and think maybe my body was trying to heal SO fast and hard, it was doing this, you know? It baffled me too, frankly. The last surgery to fix the stricture was pretty intense- he removed the sigmoid and much of the rectum, and ended up creating what was called a " colon pouch " (it's more commonly done with small intestine, not large- but in this case, with almost no 'storage space' between the colon and remaining retcum, he created the colon pouch to give me that space back- otherwise, i'd have been running to the bathroom every few minutes. UGH...) The colon pouch is created by doubling the colon onto itself and then snipping the divider and attaching the bottom of the " U " to the rectum- and the surgery went well and he reversed the illeostomy at the same time. Healing from THAT was slow! They leave the rather large hole in your belly (mine was about 3 " across and 2 " deep or so) and let it heal on it's own... but I heal fast, and that's where it is now- all healed but for the tiniest little scab and my now amazing collection of frankenstien-scars. (they run from the lowest point at the pubic bone to the highest point JUST under the breastbone. icky!) By all rights, it should be OVER. Done. Finito. ...There is a small section of stenosis, but it's less than 1/3 of the diameter of the surgery joint, so it isn't a problem enough to even mess with (lest that make it worse, you know?)... but even tho I was on my feet and home again in only a couple days, I just... I haven't come back. I'm starting to really feel it, too- the surgeries were hard but no biggie in the end... but that this didn't 'fix' everything... I just don't know what to do. A week or two after surgery, my gut was still going nuts, but you know, it had been disconnected for almost a year! ...so I was cutting that some serious slack, and not worrying... except I am just exhausted... sleep all the time, NO joke- or can't sleep at all. Nothing in between. I took a 'trazodone' on doctors orders to get some sleep after an insomnia, and I slept for three days, with only two half-our wake periods per day... hey, I like sleep, but... YIKES. No more of those! I sleep too much, even with the times I 'can't get to sleep when I want to' and I am just exhausted all the time. I feel like I have been beat on- my gut gives me a one minute warning before everything has to go or ELSE (I think the pouch fills, and then the uh, you know, potty emergency is just taking it out of me when that happens) yet again- that too is sucking the life out of me like the illeostomy never did!! (and with the illeostomy, I was so badly dehydrated once, I had a 20 day hospital stay while they got me back again! argh!) ...I sweat profusely or get shivery-cold with very little 'reason'. It doesn't seem to matter what the external temp is, my body is just going off on me, you know? I KNOW it's only been a month or so- I had the pouch/takedown surgery in the first week of April- but the whole 'being sick' thing never happened before, with all the other surgeries! I bounce back quick! ...this time... it's been hellish. My gut STILL goes nuts like this, and that has created a world of pain from hemmrhoids/fissures caused only by that irritation... I'm really having the worst time of it emotionally, because there's so many issues to think about, you know? I REALLY expected this was the 'solve' and it'd be over and done with... and before the last couple surgeries, my surgeon stopped taking the medicaid/DSHS I am stuck on, and was doing the work for free/gratis, only because he felt he'd " started it " and wanted to be the one to finish it and see me through- his attitude twords me never changed, but BOY did his office's!! ...I couldn't hardly talk to the receptionest without getting a grilling- all because I was essentially a charity case, without a way to pay... I know I can't call the office now, and go " back " , because not only would he struggle with it ethically (I'm sure anyway) but the office gal would make me crazy. I'm not an ego- type, but my pride is battered enough with the indignancy of this whole thing as it IS... this is not a fun part of the anatomy to have everyone focused on, heh!... but I can't handle this whole charity thing... it was just the final straw internally, when the problems didn't resolve. The last follow-up I had, he didn't expect any more problems, and handed me back to my general doc. The only thing is, it's been a couple weeks, and I am still REALLY suffering, and I just don't know what I should do. It's complicated- he was treating me gratis for the last bit in part because he was training a new " fellow " (surgeon coming into this specialty) and that guy is (apologies to any who might know him!) kind of a jerk. I just don't much like him, or i'd go pester HIM... but now that I am supposed to be done, and over with and everything... I don't really know how to cope with this still being a problem. I AM giving it some time, in hopes it is just everything learning how to work again (i'm sure potty-training wasn't fun the first time, why would anyone want to experience the joys of that as a 30- something'er? smirk!) ...but because I am so out of it sick too.... I just really worry that there is still something wrong... and I don't have the slightest idea how to resolve it, who to go to, or even how to handle it mentally. A LOT of folks who have 'temporary' illeostomies end up having to get one for life, and i'm not too big on that idea, frankly... tho I wouldn't die or anything if it was the only way to fix things... but while cutting a PEICE of colon (or even all the sigmoid/ect) is a big deal, I am REALLY hesitant to let them yank out the whole colon... and typically, when they do that, they don't leave everything connected, they do the permenant illeostomy... sigh. ugh. argh... So that's the HUGEly long and confusing story... there's just no polite terms for it all... but I'm running in circles inside, worrying about what I am going to do now... especially if this doesn't all settle out in the next month or so. I can't spend the rest of my life laying in bed or on the couch because I can't sit up, you know? I was that sick before... and sleeping all the time is a definate quality-of-life killer too. (smirk) ...sleep is fun, but... argh!! ...and of course, like everyone else in the world, my personal life didn't stop for the duration, so I have the kinds of regular problems a lot of folks in my position have- things that I know I could handle better if I wasn't feeling so darn SICK all the time!! I haven't the slightest idea where to turn next... or how long to wait before I try and take action, you know? How much is too much? When is it /really/ being sick and not just being whiney, pushing too hard too soon.... and am I just somehow addicted to being sick all the time or something wierd like that? (I have NO idea why that scares me, but it does. I have always hated being sick, and so far as I can tell i STILL lothe it- but what IF... you know? people have gotten addicted to wierder!) ...bah. (hey, anyone still reading definately has my respect- that is some serious spammage there!) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 5, 2003 Report Share Posted August 5, 2003 Hey Art, I am so impressed your doctor even bothered to test you for ehrlichiosis. There are doctors out here who act like they don't know what it is, oh I live in CT by the way. I sure do think you could have gotten Lyme with the ehrlich., why not? They go together, and from what it seems, the Lyme is more common (maybe that is another medical myth though). I hope you get well soon. I know there are many on this board who are not in this group, but most of the guys I know who get bit get better faster. My partner's uncle needed a couple of months of doxy, but he got over it. There are three other guys I know of personally who got better with just oral abx. The women I know however...well, they haven't fared/aren't faring as well, me included. My one big piece of advice: Follow up! Especially if you like this doctor. If you come off this abx and in a month you feel shitty again, go back and talk about different abx. If you get new symptoms, go back. If you never really feel well, go back. I spent too many months post doxy telling myself I felt unwell because I had been on abx, then I got new symptoms and they are some seriously unpleasant ones. If I had just followed up with the doctor during that early stage I might have nipped this in the bud. Take it easy, and feel better. I hope someone has some good info for you on ehrlichia. - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 6, 2003 Report Share Posted August 6, 2003 Thanks Sounds like good advice. I'm planning on going in for a follow-up late next week. I'll chime in with a progress report once in a while. Am feeling quite a bit better - only complaint now is occasional itchy spots in random locations. Also from CT, in the woods of Mdsx Cty for the past 20 years. Used to like to watch the Deer, even set out salt lick for 'em. Now when they come around I chase them away. Art -- The flower that follows the sun does so even on cloudy days. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 6, 2003 Report Share Posted August 6, 2003 Also from CT, in the woods of Mdsx Cty for the past 20 years. Used to like > to watch the Deer, even set out salt lick for 'em. Now when they come around > I chase them away. Yeah, it's sad isn't it? Best of luck, and stay on top of this. - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 2, 2004 Report Share Posted February 2, 2004 Welcome to the list. Just remenber Rod and Ross lie alot as well as drink cheap beer Cheers Tom >From: " eddiecurtin68 " <eddiecurtin@...> >Reply- > >Subject: New Guy >Date: Mon, 02 Feb 2004 12:53:16 -0000 > >Hi, my name is Eddie and I am new to your group. I am interested in >becoming a remote medic. Here is a little of my history. I served in >the Parachute Regiment for 11 years, 9 of those as a company medic. I >then transferred to the Medical Corp. to train as an Operating >Department Practitioner (ODP). I have now left the Army and I am >currently working in a hospital in Kent. Most of my work is in the >operating theatre, but I also spend some time in A & E. I have enrolled >on the off shore medics course with a company called Inter Medic in >Plymouth, has anyone got any feedback about this company. Although I >have a lot of experience I don't know what the course entails, >could >anybody give me some revision tips? >Any pointers and information would be gratefully received! >Thanks >Eddie > > > _________________________________________________________________ Check out the coupons and bargains on MSN Offers! http://shopping.msn.com/softcontent/softcontent.aspx?scmId=1418 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 2, 2004 Report Share Posted February 2, 2004 Did you make PFA, I left in 1992 and been offshore since then, put your CV with as many places as possible, try Alison Kerr at AON 01224 669005, they are looking for medic's. You will also need to do the offshore survival, if you contact the above number they might sign you up and pay for that, good luck. Regards W Clyde, Medic CLYMED@... New Guy >Date: Mon, 02 Feb 2004 12:53:16 -0000 > >Hi, my name is Eddie and I am new to your group. I am interested in >becoming a remote medic. Here is a little of my history. I served in >the Parachute Regiment for 11 years, 9 of those as a company medic. I >then transferred to the Medical Corp. to train as an Operating >Department Practitioner (ODP). I have now left the Army and I am >currently working in a hospital in Kent. Most of my work is in the >operating theatre, but I also spend some time in A & E. I have enrolled >on the off shore medics course with a company called Inter Medic in >Plymouth, has anyone got any feedback about this company. Although I >have a lot of experience I don't know what the course entails, >could >anybody give me some revision tips? >Any pointers and information would be gratefully received! >Thanks >Eddie > > > _________________________________________________________________ Check out the coupons and bargains on MSN Offers! http://shopping.msn.com/softcontent/softcontent.aspx?scmId=1418 Member Information: List owner: Ian Sharpe Owner@... Editor: Ross Boardman Editor@... ALL list admin messages (subscriptions & unsubscriptions) should be sent to the list owner. Post message: egroups Please visit our website http://www.remotemedics.co.uk Regards The Remote Medics Team Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2004 Report Share Posted March 13, 2004 HI Wayne, Nice to meet you and welcome to the forum. You've come to the right place for information on cochlear implants. I've had mine for over three years and it has definitely made positive changes in my life!! I am a volunteer and am always available to ansdwer any questions you have about the Nucleus implant and what it is like to live and hear with one. If you would like to read my implant journal please let me know and I will send it to you off the forum as it is very long. Regards! Quote Link to comment Share on other sites More sharing options...
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